510(k) K233838 · NEY System, Ablation, Microwave And Accessories
Emprint Ablation System with Thermosphere Technology (Overall System Name); Emprint Ablation Generator (CAGEN1); Emprint Ablation Generator HP (CAGENHP); Emprint Ablation Pump (CAPUMP1); Covidien™ Ablation Footswitch (RFASW); Emprint Reinforced Percutaneous Antenna 15cm (CA15L2); Emprint Reinforced
| Applicant | Medtronic, Inc., Lafayette CO, US |
| Decision | Substantially Equivalent, Mar 28, 2024 |
| Received | Dec 4, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233838
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.